Management of a pregnant patient with chylomicronemia from a novel mutation in GPIHBP1: a case report

• Үндсэн зохиолчид: Min-Huan Lin (Зохиогч), Xiao-Hui Tian (Зохиогч), Xiu-Lan Hao (Зохиогч), Hui Fei (Зохиогч), Jian-Lan Yin (Зохиогч), Dan-Dan Yan (Зохиогч), Tian Li (Зохиогч)
• Формат: Ном
• Хэвлэсэн: BMC, 2020-05-01T00:00:00Z.
• Нөхцлүүд: article
• Онлайн хандалт: Connect to this object online.

Abstract Background Familial chylomicronemia syndrome (FCS) is a rare autosomal recessive lipid disorder often associated with recurrent episodes of pancreatitis. It is documented in most cases with FCS due to the mutations of key proteins in lipolysis, including LPL, APOC2, APOA5, LMF1 and GPIHBP1....